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Benecial Eects of Moringa oleifera Seed Oil Bioactive Compounds
Mehta, L. K., Balaraman, R., Amin, A. H., Bafna, P. A., & Gulati, O. D. (2003). Effect of fruits of Moringa
oleifera on the lipid profile of normal and hypercholesterolaemic rabbits. Journal of Ethnopharmacology, 86(2-3), 191–195. doi:10.1016/S0378-8741(03)00075-8 PMID:12738086
Menendez, J. A., Vellon, L., Colomer, R., & Lupu, R. (2005). Oleic acid the main monounsaturated fatty
acid of olive oil, suppresses Her-2/neu (erbB-2) expression and synergistically enhances the growth inhibitory effects of trastuzumab (Herceptin) in breast cancer cells with Her-2/neu oncogene amplification.
Annals of Oncology: Official Journal of the European Society for Medical Oncology, 16(3), 359–371.
doi:10.1093/annonc/mdi090 PMID:15642702
Mishra, S., & Vinayak, M. (2011). Anti-carcinogenic action of ellagic acid mediated via modulation of
oxidative stress regulated genes in Dalton lymphoma bearing mice. Leukemia & Lymphoma, 52(11),
2155–2161. doi:10.3109/10428194.2011.591014 PMID:21756219
Mohammed, A. S., Lai, O. M., Muhammad, S. K. S., Long, K., & Ghazali, H. M. (2003). Moringa
oleifera, Potentially a new source of oleic acid-type oil for Malaysia. In Investing in Innovation, 3 (pp.
137–140). Serdang Press.
Monica, G. M. (2005). Miracle Tree. KOS Health Publications.
Munday, R., & Munday, C. M. (2004). Induction of phase II detoxification enzymes in ratsby plantderived isothiocyanates: Comparison of allylisothiocyanate with sulforaphane and related compounds.
Journal of Agricultural and Food Chemistry, 52(7), 1867–1871. doi:10.1021/jf030549s PMID:15053522
Nadeem, M., & Imran, M. (2016). Promising features of Moringa oleifera oil: Recent updates and per-
spectives. Lipids in Health and Disease, 15(1), 212. doi:10.118612944-016-0379-0 PMID:27931216
Ogbunugafor, H. A., Eneh, F. U., Ozumba, A. N., Igwo-Ezikpe, M. N., Okpuzor, J., Igwilo, I. O., Adenekan, S. O., & Onyekwelu, O. A. (2011). Physico-chemical and antioxidant properties of Moringa
oleifera seed oil. Pakistan Journal of Nutrition, 10(5), 409–414. doi:10.3923/pjn.2011.409.414
Oguntibeju, O. O. (2019). Type 2 diabetes mellitus, oxidative stress and inflammation: Examining the links.
International Journal of Physiology, Pathophysiology and Pharmacology, 11, 45–63. PMID:31333808
Ojiako, E. N., & Okeke, C. C. (2013). Determination of antioxidant of Moringaoleifera seed oil and its
use in the production of a body cream. Asian Journal of Plant Science & Research, 3, 1–4.
Ong, K. W., Hsu, A., & Tan, B. K. (2013). Anti-diabetic and anti-lipidemic effects ofchlorogenic acid
are mediated by AMPK activation. Biochemical Pharmacology, 85(9), 1341–1351. doi:10.1016/j.
bcp.2013.02.008 PMID:23416115
Opie, L. H., Cammerford, P. J., Gerch, B. J., & Pfeffer, M. A. (2006). Controversies in ventricular remodeling. Lancet, 367(9507), 356–367. doi:10.1016/S0140-6736(06)68074-4 PMID:16443044
Pandey, K. B., & Rizvi, S. I. (2009). Plant polyphenols as dietary antioxidants in human health and disease.
Oxidative Medicine and Cellular Longevity, 2(5), 270–278. doi:10.4161/oxim.2.5.9498 PMID:20716914
Park, S. H., Kim, J. L., Lee, E. S., Han, S. Y., Gong, J. H., Kang, M. K., & Kang, Y. H. (2011). Dietary
ellagic acid attenuates oxidized LDL uptake and stimulates cholesterol efflux in murine macrophages.
The Journal of Nutrition, 141(11), 1931–1937. doi:10.3945/jn.111.144816 PMID:21940512
288
EBSCOhost - printed on 2/13/2023 11:18 AM via . All use subject to https://www.ebsco.com/terms-of-use

Benecial Eects of Moringa oleifera Seed Oil Bioactive Compounds
Pauwels, E. K. J. (2011). The protective effect of the mediterranean diet: Focus on cancer and cardiovascular risk. Medical Principles and Practice, 20(2), 103–111. doi:10.1159/000321197 PMID:21252562
Pechanova, O., Bernatova, I., Babal, P., Martínez, M. C., Kyselá, S., Stvrtina, S., & Andriantsitohaina,
R. (2004). Red wine polyphenols prevent cardiovascular alterations in L-NAME-induced hypertension.
Journal of Hypertension, 22(8), 1551–1559. doi:10.1097/01.hjh.0000133734.32125.c7 PMID:15257179
Pereira, F. S. G., Galvao, C. C., de Lima, V. F., da Rocha, M. F. A., Schuler, A. R. P., & da Silva, V. L.
(2016). The versatility of the Moringa oleifera oil in sustainable applications. Oilseeds and Fats Crops
and Lipids, 23(6), 1-7.
Pinho, E., Ferreira, I. C., Barros, L., Carvalho, A. M., Soares, G., & Henriques, M. (2014). Antibacterial potential of northeastern portugal wild plant extracts and respective phenolic compounds. BioMed
Research International, 2014, 814590. doi:10.1155/2014/814590 PMID:24804249
Prasad, C. N., Anjana, T., Banerji, A., & Gopalakrishnapillai, A. (2010). Gallic acid induces GLUT4
translocation and glucose uptake activity in 3T3-L1 cells. FEBS Letters, 584(3), 531–536. doi:10.1016/j.
febslet.2009.11.092 PMID:19962377
Psaltopoulou, T., Naska, A., Orfanos, P., Trichopoulos, D., Mountokalakis, T., & Trichopoulou, A.
(2004). Olive oil, the Mediterranean diet, and arterial blood pressure: The Greek European Prospective
Investigation into Cancer and Nutrition (EPIC) study. The American Journal of Clinical Nutrition, 80(4),
1012–1018. doi:10.1093/ajcn/80.4.1012 PMID:15447913
Quideau, S., Deffieux, D., Douat-Casassus, C., & Pouységu, L. (2011). Plant polyphenols: Chemical
properties, biological activities, and synthesis. Angewandte Chemie International Edition, 50(3), 586–621.
doi:10.1002/anie.201000044 PMID:21226137
Rahman, I. M. M., Barua, S., Nazimuddin, M., Begum, Z. A., Rahman, M. A., & Hasegawa, H. (2009).
Physicochemicalproperties of Moringa oleifera Lam. seed oil of the indigenous-cultivar of Bangladesh.
Journal of Food Lipids, 16(4), 540–553. doi:10.1111/j.1745-4522.2009.01165.x
Ras, R. T., Geleijnse, J. M., & Trautwein, E. A. (2014). LDL-cholesterol-lowering effect of plant sterols and stanols across different dose ranges: A meta-analysis of randomised controlled studies. British
Journal of Nutrition, 112(2), 214–219. doi:10.1017/S0007114514000750 PMID:24780090
Reddy, L., Odhav, B., & Bhoola, K. D. (2003). Natural products for cancer prevention: A global perspective. Pharmacology & Therapeutics, 99(1), 1–13. doi:10.1016/S0163-7258(03)00042-1 PMID:12804695
Rhein, L. D., & Fluhr, J. W. (2010). Aging Skin: Current and Future Therapeutic Strategies. Allured
Business Media.
Rocha, L. D., Monteiro, M. C., & Teodoro, A. J. (2012). Anticancer properties of hydroxycinnamic
acids – a review. Journal of Cancer Research and Clinical Oncology, 1, 109–121.
Rodeiro, I., Donato, M. T., Jimenez, N., Garrido, G., Molina-Torres, J., Menendez, R., Castell, J. V., &
Gómez-Lechón, M. J. (2009). Inhibition of human p 450 enzymes bynatural extracts used in traditional
medicine. Phytotherapy Research, 23(2), 279–282. doi:10.1002/ptr.2613 PMID:18844254
EBSCOhost - printed on 2/13/2023 11:18 AM via . All use subject to https://www.ebsco.com/terms-of-use
289

Benecial Eects of Moringa oleifera Seed Oil Bioactive Compounds
Sales-Campos, H., Reis de Souza, P., Crema Peghini, B., Santana da Silva, J., & Ribeiro Cardoso, C.
(2013). An Overview of the Modulatory Effects of Oleic Acid in Health and Disease. Mini-Reviews in
Medicinal Chemistry, 13(2), 201–210. PMID:23278117
Samoylenko, A., Hossain, J. A., Mennerich, D., Kellokumpu, S., Hiltunen, J. K., & Kietzmann, T.
(2013). Nutritional countermeasures targeting reactive oxygen species in cancer: From mechanisms to
biomarkers and clinical evidence. Antioxidants & Redox Signaling, 19(17), 2157–2196. doi:10.1089/
ars.2012.4662 PMID:23458328
Sánchez-Machado, D. I., Nùñez-Gastelum, J. A., Reyes-Moreno, C., Ramírez-Wong, B., & LópezCervantes, J. (2010). Nutritional quality of edible parts of Moringaoleifera. Food Analytical Methods,
3(3), 175–180. doi:10.100712161-009-9106-z
Sandhya, B., Thomas, S., Isabel, W., & Shenbagarathai, R. (2006). Ethnomedicinal plants used by the
Valaiyan community of Piranmalai Hills (Reserved Forest), Tamil Nadu, India. A pilot study. African
Journal of Traditional, Complementary, and Alternative Medicines, 3(1), 101–114.
Schwingshackl, L., & Hoffmann, G. (2014). Monounsaturated fatty acids, olive oil and health status:
A systematic review and meta-analysis of cohort studies. Lipids in Health and Disease, 13(1), 154.
doi:10.1186/1476-511X-13-154 PMID:25274026
Słoczynska, K., Powroznik, B., Pekala, E., & Waszkielewicz, A. M. (2014). Antimutagenic compounds
and their possible mechanisms of action. Journal of Applied Genetics, 55(2), 273–285. doi:10.100713353-
014-0198-9 PMID:24615570
Souza, H. C. D., Ballejo, G., Salgado, M. C. O., Dias Da Silva, V. J., & Salgado, H. C. (2001). Cardiac sympathetic overactivity and decreased baroreflex sensitivity in L-NAME hypertensive rats.
American Journal of Physiology. Heart and Circulatory Physiology, 280(2), 844–850. doi:10.1152/
ajpheart.2001.280.2.H844 PMID:11158985
Teres, S., Barcelo-Coblijn, G., Benet, M., Alvarez, R., Bressani, R., Halver, J. E., & Escriba, P. V. (2008).
Oleic acid content is responsible for the reduction in blood pressure induced by olive oil. Proceedings of
the National Academy of Sciences of the United States of America, 105(37), 13811–13816. doi:10.1073/
pnas.0807500105 PMID:18772370
Tsaknis, J., Lalas, S., Gergis, V., Dourtoglou, V., & Spiliotis, V. (1999). Characterisation of Moringa
oleifera Variety Mbololo seed oil of Kenya. Journal of Agricultural and Food Chemistry, 47(11),
4495–4499. doi:10.1021/jf9904214 PMID:10552840
Tsaknis, J., Lalas, S., Gergis, V., & Spiliotis, V. (1998). A total characterisation of Moringa oleifera
Malawi seed oil. La Rivista Italiana delle Sostanze Grasse, 75, 21–27.
Verma, S., & Singh, S. P. (2008). Current and future status of herbal medicines. Veterinary World, 1(11),
347–350. doi:10.5455/vetworld.2008.347-350
Visioli, F., Bogani, P., Grande, S., & Galli, C. (2005). Mediterranean food and health: Building human
evidence. Journal of Physiology and Pharmacology, 56, 37–49. PMID:15800384
290
EBSCOhost - printed on 2/13/2023 11:18 AM via . All use subject to https://www.ebsco.com/terms-of-use

Benecial Eects of Moringa oleifera Seed Oil Bioactive Compounds
Wijendran, V., & Hayes, K. C. (2004). Dietary Ω-6 and Ω-3 fatty acid balance and cardiovascular health.
Annual Review of Nutrition, 24(1), 597–615. doi:10.1146/annurev.nutr.24.012003.132106 PMID:15189133
Wu, T., He, M., Zang, X., Zhou, Y., Qiu, T., Pan, S., & Xu, X. A. (2013). Structure-activity relationship
study of flavonoids as inhibitors of E. coli by membrane interaction effect. Biochimica et Biophysica Acta
(BBA) -. Biomembranes, 1828(11), 2751–2756. doi:10.1016/j.bbamem.2013.07.029 PMID:23938956
Wu, Y., Ding, Y., Tanaka, Y., & Zhang, W. (2014). Risk factors contributing to type 2diabetes and recent
advances in the treatment and prevention. International Journal of Medical Sciences, 11(11), 1185–1200.
doi:10.7150/ijms.10001 PMID:25249787
Xu, M., Zhou, H., Tan, K. C. B., Guo, R., Shiu, S. W. M., & Wong, Y. (2009). ABCG1 mediated oxidized
LDL-derived oxysterol efflux from macrophages. Biochemical and Biophysical Research Communica-
tions, 390(4), 1349–1354. doi:10.1016/j.bbrc.2009.10.152 PMID:19895785
Yang, Q., Alemany, R., Casas, J., Kitajka, K., Lanier, S. M., & Escriba, P. V. (2005). Influence of the
membrane lipid structure on signal processing via G protein-coupled receptors. Molecular Pharmacol-
ogy, 68(1), 210–217. doi:10.1124/mol.105.011692 PMID:15837842
Yaseen, G., Ahmad, M., Sultana, S., Alharrasi, A. S., Hussain, J., Zafar, M., & Ur-Rehman, S. (2015).
Ethnobotany of medicinal plants in the thar desert (Sindh) of Pakistan. Journal of Ethnopharmacology,
163, 43–59. doi:10.1016/j.jep.2014.12.053 PMID:25617748
Yoshida, Y., & Niki, E. (2003). Antioxidant effects of phytosterol and its components. Journal of Nutri-
tional Science and Vitaminology, 49(4), 277–280. doi:10.3177/jnsv.49.277 PMID:14598915
Yu, J. (2009). Study on extraction method and hypolipidemic effect on Moringa oleifera seed oil. Kun-
ming Medical University.
Yue, P., Chen, Z., Nassir, F., Bernal-Mizrachi, C., Finck, B., Azhar, S., & Abumrad, N. A. (2010).
Enhanced hepatic apoA-I secretion and peripheral efflux of cholesterol and phospholipid in CD36 null
mice. PLoS One, 5(3), e9906. doi:10.1371/journal.pone.0009906 PMID:20360851
Zambon, D., Sabate, J., Munoz, S., Campero, B., Casals, E., Merlos, M., Laguna, J. C., & Ros, E.
(2000). Substituting walnuts for monounsaturated fat improves the serum lipid profile of hypercholesterolemic men and women. A randomized crossover trial. Annals of Internal Medicine, 132(7), 538–546.
doi:10.7326/0003-4819-132-7-200004040-00005 PMID:10744590
Zang, L. Y., Cosma, G., Gardner, H., Shi, X., Castranova, V., & Vallyathan, V. (2000). Effect of antioxidant protection by ρ-coumaric acid on low-density lipoprotein cholesterol oxidation. American Journal
of Physiology. Cell Physiology, 279(4), 954–960. doi:10.1152/ajpcell.2000.279.4.C954 PMID:11003575
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291

292
Chapter 14
Bioactive Compounds of
Cucurbitaceae Seed Oils as
Nutraceuticals and Health-
Promoting Substances
Leila Rezig
https://orcid.org/0000-0002-6243-5742
High Institute of Food Industries, Tunisia
Karima Gharsallah
Faculty of Science of Tunis, Tunisia
Nesrine Mahfoudhi
University of Kairouan, Tunisia
ABSTRACT
Edible oils are one of the important products that have lately come to light for their beneficial and
nutritional properties. As a result, scientists and the oil industry are always working to demonstrate
the health-giving benefits of both fruit and vegetable seed oils. Fruits are popular for their fleshy parts.
However, the seeds are often discarded since they are thought worthless. This research looked at the
bioactive components found in Cucurbitaceae (Cucurbita spp., Cucumis melo L., Citrullus lanatus) seed
oils extracted using various extraction procedures on Cucurbitaceae seeds from various species and
geographical places throughout the globe. The outcomes of the study show that Cucurbitaceae seed oils
are a good source of nutrients and may be classified as health-promoting compounds. The discoveries
have also cleared the way for the use of these seed oil resources in the production of a broad variety of
therapeutic products.
DOI: 10.4018/978-1-6684-5129-8.ch014
Copyright © 2022, IGI Global. Copying or distributing in print or electronic forms without written permission of IGI Global is prohibited.
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Bioactive Compounds of Cucurbitaceae Seed Oils as Nutraceuticals and Health-Promoting Substances
INTRODUCTION
The scarcity of food resources, especially edible oils and fats, has forced an investigation into the potential
of current edible oil sources. Fats and oils are a significant element of practically every civilization’s
diet. They are used in cooking, frying, baking, and so forth. Fats and oils have a significant nutritional
function in the body. They provide a rich source of energy, fat-soluble vitamins, essential fatty acids,
flavor transporters, and numerous bioactive chemicals that are required for various physiological activities. The seed oils have a broad variety of bioactivities, including antioxidant, antibacterial, and
antiproliferative effects. Cucurbita crops are among the most frequent food items and raw materials
used in the production of a broad variety of dietetic, medicinal, and preventive products (Piskunova
and Mutyeva, 2016). Cucurbit seed oil is one of the most well-known products in the modern healthy
nutrition market, particularly in Austria (Piskunova, 2015; Piskunova and Mutyeva, 2016). This oil is
also gaining popularity in Russia and the former Soviet Union (Piskunova and Mutyeva, 2016). The use
of cucurbit seed oil as a healthy diet component as well as for medicinal purposes is gaining popularity
in China and Japan (Caili et al., 2006; Nishimura et al., 2014; Yao et al., 2019). The cucurbit seed oil
is high in phytosterols, with β-sitosterol accounting for more than 39% of the total, and in carotenoids,
with β-carotene and lutein being the primary components (Piskunova & Mutyeva, 2016; Ayyildiz et
al., 2019; Piskunova, 2015; Yao et al., 2019). It is regarded as a one-of-a-kind treatment for preventing
cardiovascular disease, hypertension, urogenital system disorders (prostatitis therapy), oncological and
dermatological diseases (Orsavovà et al., 2015). At the moment, there is an increasing need for medications made from natural substances, such as Cucurbitaceae seed oil. In compared to synthetic and
semi-synthetic analogs, such medications are often more effective, safer, and less expensive (Bardaa et
al., 2016; Piskunova & Mutyeva, 2016; Safar, 2019). The current chapter discusses the primary phytochemicals found in Cucurbitaceae seed oils produced by cold pressing or other methods, as well as their
positive effects in promoting health and avoiding illness.
CUCURBITACEAE SEEDS AS POTENTIONAL SOURCES
OF NEW TRENDS OF PLANT OILS
Cucurbitaceae seeds are considered as a rich source of oil (Al-Khalifa, 1996). The quantity of oil in
the seeds is determined by a range of variables, including varietal and environmental conditions. The
oil content of Cucumis melo seeds varied from 28.44 percent to 49.4 percent of dry weight (Rashwan
et al., 1993; De Melo et al., 2000; Mallek-Ayadi et al., 2019; Rezig et al., 2019). Furthermore, for the
species Citrullus lanatus, this concentration varied between 19.23 percent and 24.6 percent of the dry
weight in watermelon seeds (Al-Khalifa, 1996; Rezig et al., 2019). For the Cucurbita pepo species,
pumpkin seeds contain between 29.33 percent and 51.01 percent oil by dry weight (El-Adawy & Taha,
2001; Nyam et al., 2009; Meru et al., 2018; Rezig et al., 2019). Furthermore, for the species Cucurbita
moschata, the oil content is around 44.42 percent of the dry weight (Al-Khalifa, 1996). Applequist et
al. (2006) showed that the oil content in seeds ranged from 24.2 percent to 42.33 percent of dry weight
for the species Cucurbita maxima.
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Bioactive Compounds of Cucurbitaceae Seed Oils as Nutraceuticals and Health-Promoting Substances
Extraction and Processing of Cucurbitaceae Seed Oils
The quantity of oil extracted from Cucurbitaceae seeds varies depending on plant type, growing environment, ripening stage, seed harvesting time, and extraction technique used (Nyam et al., 2009). Organic
solvents are commonly used to extract lipids from oilseeds, but solvent extraction has some drawbacks,
including the risk of thermal degradation of unsaturated fatty acids and functional compounds depending on the extracting conditions used, as well as the need to remove the organic solvent’s residues from
the oil (Bozan & Temelli, 2002).
Mechanical cold extraction of oils using an expeller is mostly utilized for fiber-rich sources with oil
concentration more than 20%. However, as compared to solvent extraction, the expeller generally yields
a lower extraction yield (10% -18% of the oil) (Carr, 1989). It is worth noting that in both cases, plant
seed moisture should be reduced by sun-drying to facilitate extraction procedures.
To the best of our knowledge, the soxhlet device is the most often used method of extracting oil from
Cucurbitaceae seeds. Nonpolar solvents such as n-hexane and chloroform are frequently used in such
extraction techniques rather than petroleum ether (Al-Khalifa, 1996; Mariod et al., 2009; Nehdi et al.,
2013). According to reports, the solvent/kernel ratio, rather than time and temperature, has the greatest
influence on oil yield (Sultana & Ashraf, 2019).
Fatty Acid Composition and High Nutritional value
factors of Cucurbitaceae seed oils
Fatty acid Composition
Cucurbitaceae (pumpkin, melon, and watermelon) seed oils are members of the oleic-linoleic acid group
of oils, which also includes maize, sesame, sunflower, soya, and cottonseed oils. Table 1 summarizes the
proximate fatty acid content of pumpkin seed oil (PSO), melon seed oil (MSO), and watermelon seed oil
(WSO). Linoleic, oleic, palmitic, and stearic acids are the oil’s primary fatty acids. Cucurbitaceae seed
oils are a good supply of important fatty acids because to their high linoleic acid concentration. Numerous studies have shown a substantial link between dietary linoleic acid and blood cholesterol levels. A
linoleic acid-rich diet helps to decrease plasma cholesterol and lowers the risk of cardiovascular disease
(Heine et al., 1989; Horrobin & Huang, 1987). Furthermore, linoleic acid is required for the synthesis
of vitamin D, cellular membranes, and some hormones (Fruhwirth & Hermetter, 2007). Louheranta et
al. (1996), on the other hand, proposed that a high linoleic acid consumption enhances the susceptibility
of atherogenic lipoproteins to oxidation in males.
Minor bioactive lipids in Cucurbitaceae seed oils as
nutraceuticals and health promoting substances
Sterols
Phytosterols are common components of plant cell walls. Because of their structural closeness to cholesterol, they inhibit cholesterol absorption from the stomach when consumed with plant meals. Purified
plant sterols or stanols have been added to a variety of meals in recent decades to create functional foods
with exceptional hypocholesterolemic action. According to Marangoni & Poli (2010), a daily consumption
294
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Bioactive Compounds of Cucurbitaceae Seed Oils as Nutraceuticals and Health-Promoting Substances
Table 1. Fatty acid (%) composition of Cucurbitaceae seed oils.
Cucurbita maxima Cucurbita pepo
Rezig et
al. (2012)
Myristic acid
(C14:0)
Palmitic acid
(C16:0)
Stearic acid (C18:0)
Oleic acid (C18:1)
Linoleic acid
(C18:2)
Linolenic acid
(C18:3)
Arachidonic acid
(C20:0)
Gondoic acid
(C20:1)
% Saturated fatty
acids (SAFA)
% Monounsaturated
fatty acids (MUFA)
% Polyunsaturated
fatty acids (PUFA)
a
: Seed oil obtained by cold extraction in petroleum ether;b: Cold-pressed seed oil; c: Supercritical CO2 extraction; d: Seed oil obtained
-
15.97
± 0.39
4.68 ±
44.11
± 0.63
34.77
± 0.95
tr. - 0.2 ± 0.22
0.41 ±
- - - - - -
21.07
± 1.19
44.12
± 0.57
34.78
± 0.85
0.56
0.40
Rezig et
a
0.12 ±
16.17
8.57 ±
30.56
43.86
0.60 ±
25.48
30.67
43.86
al. (2018)
0.00
± 2.32
0.65
± 2.87
± 5.24
0.04
± 2.33
± 2.78
± 2.36
Rabrenović,
b
et al. (2013)
- - 0.16 tr.
11.2 ± 0.02
5.2 ± 0.08
39.2 ± 0.10
44.5 ± 0.15
- - 0.17
16.4 ± 0.10
39.2 ± 0.69
44.7 ± 0.78
b
Salgin
and Kormaz
(2011)
9.59 ±
7.46 ±
32.35
± 0.85
48.48
± 0.63
0.60 ±
17.05
± 1.49
32.35
± 0.85
49.08
± 0.83
0.94
0.55
0.20
Cucurbita
moschata
Al-
c
Khalifa (1996)
13.1 14.43 ± 1.51
6.0 5.81 ± 0.62
26.2 23.52 ± 2.94
53.2 59.26 ± 6.54
0.12 0.22
19.71 20.24 ± 3.12 5.79
26.64 23.52 ± 2.94 16.23
53.33 59.48 ± 6.34 69.18
Cucumis melo Citrullus lanatus
var.
‘Ananas’
Rezig et
d
al., (2019)
0.24 ±
0.02
Mallek-
b
var.
‘Maazoun’
Ayadi et al.
e
(2012)
0.04 ±
0.01
8.76 ±
0.07
5.64 ±
0.06
15.84
± 0.03
68.98
± 0.05
0.20 ±
0.00
0.16 ±
0.01
0.26 ±
0.01
var.
‘Ananas’
Rezig et
al., (2019)
tr.
9.88 ±
0.86
6.96 ±
0.71
14.25 ±
1.56
68.07 ±
7.56
tr.
0.26 ±
0.03
tr.
17.10 ±
1.85
14.25 ±
1.87
68.07 ±
7.89
b
Górnaś
& Rudzińska
(2016)
0.05 ±
0.00
10.48 ±
0.06
7.37 ±
0.05
14.80 ±
0.09
66.42 ±
0.18
0.19 ±
0.00
0.31 ±
0.01
0.10 ±
0.00
-
-
-
by cold extraction in chloroform/methanol 2:1; e: Seed oil obtained by cold extraction in hexane. SAFA: Saturated fatty acids; MUFA:
Monounsaturated fatty acids; PUFA: Polyunsaturated fatty Acids; tr.: trace amounts (less than 0.2%). Values are means ± SD of three
determinations; SD: standard deviation.
e
of plant sterols or stanols of 1.6-2 g/day, which are found in these foods, may lower cholesterol absorption from the gut by roughly 30% and plasma LDL cholesterol levels by 8-10%. Because the impact of
plant sterols or stanols on plasma LDL cholesterol is additive to that of statins, the former may be used
to boost the latter’s hypocholesterolemic action in individuals who need a significant decrease in plasma
LDL cholesterol levels. Phytosterols, at doses of up to 3 g per day, are both safe and effective cholesterollowering agents. Among the several plant sterols, β-sitosterol has received the most attention in terms
of its physiological impact on human health. Many investigations have so proved sitosterol’s beneficial
qualities (Yang et al., 2001). This phytochemical molecule is presently on the market and has been scientifically demonstrated to decrease low-density lipoprotein (LDL) cholesterol by 10% to 15% as part
of a balanced diet (Ntanios, 2001). Rezig et al. (2019) reported a sterol content in “Ananas” variation
of the Tunisian plant Cucumis melo L., belonging to the Cucurbitaceae family, of 5162 mg/kg oil. This
content was higher in the cold pressed seed oil than in the “Maazoun” Cucumis melo L. and honeydew
melon (Cucumis melo) seed oils found by Mallek-Ayadi et al. (2018) and Górnaś & Rudzińska (2016),
respectively, and lower than that found by Veronezi & Jorge (2018) in the Cucumis melo var. “inodorus”
seed oil obtained by n-hexane extraction. The primary sterols were β-sitosterol and Δ5-avenasterol,
which accounted for 92.6 percent of total sterols in melon seed oil. β-sitosterol was also found in the
seed oils of Cucurbita maxima var. “Béjaoui,” Cucurbita pepo L., Kalahari melon (Citrullus lanatus),
Bittermelon (Momordica charantia L.), Cucumis melo L., and watermelon (Citrullus lanatus (Thunb.)
Matsum. & Nakai)
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295

Bioactive Compounds of Cucurbitaceae Seed Oils as Nutraceuticals and Health-Promoting Substances
Tocopherols and tocotrienols (tocochromanols)
Tocopherols and tocotrienols, abbreviated as tocols, are natural lipophilic antioxidants that preserve vegetable oils from oxidation (Ozcan et al., 2019; Schwartz et al., 2008). Tocols (vitamin E) are composed
of a chromanol ring with a C16 phytol side chain and are divided into two forms based on whether the
side chain is saturated (tocopherols) or has three double bonds at carbons 3, 7, and 11 (tocotrienols)
(Lachman et al., 2018). Tocopherols and tocotrienols occur in four isomers known as alpha, beta, gamma,
and delta; they vary in the methylation pattern of the benzopyran ring, which has three methyl groups (at
C-5, C-7, and C-8) (Boschin & Arnoldi, 2011). The most potent lipid-soluble antioxidants in vegetable
oils are alpha and gamma tocopherols. The strongest vitamin E activity is shown by alpha-tocopherol,
whereas the highest antioxidant activity is shown by gamma-tocopherol (Böhmdorfer et al., 2011; Boschin
& Arnoldi, 2011). Recently, there has been a surge in interest in extracting oils from fruit seeds. The
bulk of earlier research on fruit seed oils focused only on the fatty acid content. Similarly, there is little
information on the profile of tocochromanols, particularly those identified in Cucrubitaceae seed oils.
Table 27. 2a shows the tocopherol and tocotrienol compositions of Citrullus lanatus seed oils recovered
using solvent and compression extraction procedures.
According to Górnaś et al. (2014), γ-T tocochromanol predominated in Citrullus lanatus (Thunb.)
Matsum & Nakai seed oil, with a concentration 25 times greater than that found for α-T. Nonetheless,
watermelon seeds contained trace quantities of β-T, γ-T, α-T3, and γ-T3. Similarly, only a high level of
α-T and a low quantity of δ-T were discovered in the seeds of four distinct watermelon cultivars cultivated
in Pakistan (Raziq et al., 2012). However, Górnaś et al. (2014) discovered a comparable tocochromanol
composition in Kalahari melon seeds from northern Namibia and Citrullus lanatus (Thunb.) Matsum &
Nakai seeds from Brazil (Nyam et al., 2009; de Conto et al., 2011). The high amount of γ- tocopherol
is consistent with the findings of Mariod et al. (2009), Jorge et al. (2015), and Angelova-Romova et al.
(2019). They all claimed that γ-tocopherol was the dominant nutrient. According to Rossel (1991), the
-1
initial content of tocopherols may range from a few mg kg
oil type and fatty acid composition. It should be noted that there is relatively little information available
on the tocopherol content of cold pressed watermelon seeds. According to our knowledge, de Conto et
al. (2011) were the first to compare the tocopherol concentrations of watermelon seeds extracted chemically by solvent and mechanically by an expeller. The authors also stated that the extraction process
had no effect on the preservation of beneficial components such tocopherols (p ≤ 0.05). Table 27. 2b
shows the tocopherol and tocotrienol content of Cucumis melo L. seed oils derived by solvent extraction
techniques and accessible in the literature.
As shown, γ-tocopherol was the most abundant tocopherol in all samples, accounting for 78.21 percent
and 100 percent of total tocopherols in the Cucumis melo var. ‘Agrestis’ coming from Gezira in Sudan,
and in the same variety; whose fruits were purchased from a local market in Khartoum North (Sudan)
respectively (Azhari et al., 2014; Mariod et al., 2009). Petkova & Antova (2019) corroborated the discov-
ery in melon seed oil, where γ-tocopherol accounted for 87.8 percent of total tocopherols. According to
Fatnassi et al. (2009), α-tocopherol is suggested for human and animal consumption since it has greater
biological activity than other tocopherols. However, γ-tocopherol has a stronger antioxidant capacity
than α-tocopherol. The total tocols content of pumpkin seed oil ranges from 265.7 mg/kg to 977.9 mg/
kg (Akin et al., 2018; Vujasinovic et al., 2012). The predominant tocopherol isomer is γ-tocopherol,
which accounts for over 90% of total tocopherols in cold pressed pumpkin seed oil. This tocopherol
isomer’s concentration may vary between 251 mg/kg and 775 mg/kg. α-tocopherol is the second most
to several hundred mg kg-1 depending on the
296
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Bioactive Compounds of Cucurbitaceae Seed Oils as Nutraceuticals and Health-Promoting Substances
prevalent tocol, with concentrations ranging from 10.1 mg/kg to 353 mg/kg (Broznić et al., 2016; Naziri
et al., 2016). Pumpkin seed oil contains trace levels of β- and δ-tocopherols (Rabrenović et al., 2014;
Vujasinovic et al., 2012). In addition to tocopherols, cold pressed oils of pumpkin seeds cultivated in
Turkey included α-, β-, and γ-tocotrienols (Akin et al., 2018). While Naziri et al. (2016) proposed that
α- and γ-tocopherol increase the oxidative stability of pumpkin seed oil, Gorjanović et al. (2011) found
strong positive correlations between δ-tocopherol content and DPPH and H
-scavenging activities of
2O2
cold pressed pumpkin seed oil (r = 0.89 and r = 0.87, respectively).
Phenolic Compounds
In recent years, there has been an increase in interest in researching phenolic chemicals derived from
oilseeds, their skins, hulls, and oil cake meals. This interest stems from the fact that these chemicals have
the ability to improve one’s health (Peschel et al., 2006; Wang et al., 2007). Vanillic acid (11.4 g/100
g), p-coumaric acid (3.8 g/100 g), ferulic acid (3.8 g/100 g), and protocatechuic acid (3.1 g/100 g) were
found in Cucurbita pepo seed oil by Siger et al. (2008). Furthermore, Rezig et al. (2012) discovered
six phenolic acids in Cucurbita maxima var. “Béjaoui” seed oil extracted by petroleum ether: syringic
acid (7.96 mg/100g), ferulic acid (4.99 mg/100g), caffeic acid (3.88 mg/100g), p-coumaric acid (2.5
mg/100g), vanillic acid (2.46 mg/100g), and protocatechuic acid (1.81 mg/100g). Caffeic acid (3.4 - 3.8
mg/100 g) and syringic acid (7.6 - 8 mg/100 g) were found in pumpkin seed oils derived from Turkey
seeds, according to Akin et al. (2018). Regarding watermelon seed oil, Rezig et al. (2019) discovered
two kinds of phenolic chemicals, including phenolic acids and lignans, in the cold pressed var. “Cris-
mon” seed oils, which are represented by caffeic acid (1.33 mg/g) and pinoresinol (1.02 mg/g). Caffeic
acid (0.41 mg/100g) was found in melon seed oil by Nyam et al. (2009), followed by vanillic acid (0.55
mg/100g), gallic acid (0.23 mg/100g), p-hydroxybenzoic acid (0.21 mg/100g), p-coumaric acid (0.18
mg/100g), ferulic acid (0.17 mg/100g), and protocatechuic acid (0.05 mg/100g).
Total Phenolics and Flavonoid Contents
The total phenolic and flavonoid content of Cucurbitaceae seed oils is little documented in the scientific
literature. Hashemi et al. (2017) found watermelon Citrullus lanatus seed oil to have a total phenolic
content (TPC) of 111 mg gallic acid equivalent (GAE) per kilogram of oil. This level was lower than
that found in Citrullus lanatus seed oil (1428.9 mg GAE/kg), Cucumis melo “Maazoun” variety (226 mg
GAE/Kg), and yellow melon (Cucumis melo var. ‘inodorus Naudin’) (130.7 mg GAE/kg) (da Silva &
Jorge, 2014; Jorge et al., 2015; Mallek-Ayadi et al., 2019). TPC variations may be related to variations
in Cucurbitaceae cultivars, growth circumstances, and the polarity of the extraction solvents (Rahman
et al., 2013). When compared to soybean, sunflower, rapeseed, maize, grapeseed, hemp, flax, and rice
bran cold pressed oils, pumpkin seed oil has a significantly high TPC (Siger et al., 2008). TPC levels in
pumpkin seeds ranged from 4.63 mg GAE/kg to 2240 mg GAE/kg (Aktaş et al., 2018; Vujasinovic et
al., 2012). Flavonoids, on the other hand, are the most frequent and extensively dispersed plant phenolic
chemical group. They are essential for plant development and protection against infection and injury.
Because of their considerable antioxidant and chelating characteristics, these plant secondary metabolites
have been found to have a broad spectrum of antiallergic, antiinflammatory, antibacterial, and antican-
cer actions (Heim et al., 2002; Khatiwor et al., 2010). Morais et al. (2015) found 24.7 mg quercetin
equivalent (QE) and 3.61 mg QE per 100g of dry weight seeds in watermelon (Citrullus lanatnus) and
297
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